A multi-omics analysis unveils functional and regulatory links between hydroxybenzene and aromatic amino acid metabolism in <i>Candida albicans</i>

The opportunistic human fungal pathogen <i>Candida albicans</i> possesses a remarkable metabolic plasticity, which is essential for both fungal commensalism and virulence and influences its physiology and behavior in multiple ways. The investigation of such processes particularly benefits from the emergence of multi-omics and <i>in silico</i> approaches. In this study, we combined a multi-omics approach with genome-scale metabolic modeling to investigate the fungal metabolic adaptation to amino acid utilization and starvation. Most strikingly, we found an altered activity of the shikimate pathway upon amino acid starvation, accompanied by a simultaneous induction of two metabolic gene clusters required for the metabolism of hydroxybenzenes. Further analyses revealed so far unknown potential functional and regulatory links between both metabolic pathways, which provide starting points for future research leading to a better understanding of the fungal adaptation to dynamic host conditions.

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Journal
mSystems
Published
2025-10-08
DOI
https://doi.org/10.1128/msystems.00226-25
Primary Topic
Antifungal resistance and susceptibility
Type
article
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article

A multi-omics analysis unveils functional and regulatory links between hydroxybenzene and aromatic amino acid metabolism in Candida albicans

Gianni Panagiotou, Bernhard Hube, Sascha Schäuble, Slavena Vylkova et al.
mSystems
Antifungal resistance and susceptibility
article

A multi-omics analysis unveils functional and regulatory links between hydroxybenzene and aromatic amino acid metabolism in Candida albicans

Gianni Panagiotou, Bernhard Hube, Sascha Schäuble, Slavena Vylkova, Osama Elshafee, Dominik Driesch, Bettina Böttcher, Enrico Garbe, Tim B Schille, Robert L. Jesse, Lasse van Wilijck
article en

Abstract

The opportunistic human fungal pathogen <i>Candida albicans</i> possesses a remarkable metabolic plasticity, which is essential for both fungal commensalism and virulence and influences its physiology and behavior in multiple ways. The investigation of such processes particularly benefits from the emergence of multi-omics and <i>in silico</i> approaches. In this study, we combined a multi-omics approach with genome-scale metabolic modeling to investigate the fungal metabolic adaptation to amino acid utilization and starvation. Most strikingly, we found an altered activity of the shikimate pathway upon amino acid starvation, accompanied by a simultaneous induction of two metabolic gene clusters required for the metabolism of hydroxybenzenes. Further analyses revealed so far unknown potential functional and regulatory links between both metabolic pathways, which provide starting points for future research leading to a better understanding of the fungal adaptation to dynamic host conditions.

mSystemsVol. 10(11)
Institut Pasteur (FR), University of California, San Francisco (US), Schiller International University (FR), Université Paris Cité (FR), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) (DE), Friedrich Schiller University Jena (DE)
Openalex Percentile: Top 67%
Antifungal resistance and susceptibility
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